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Mechanism of activation

Mechanism of activation. Models for mechansim of activation. Direct contact between an activator and RNA polymerase or GTF Indirect interactions Adaptor Mediator Histone modifier complexes Nucleosome remodelers No contact between enhancer bound proteins and the target promoter

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Mechanism of activation

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  1. Mechanism of activation

  2. Models for mechansim of activation • Direct contact between an activator and RNA polymerase or GTF • Indirect interactions • Adaptor • Mediator • Histone modifier complexes • Nucleosome remodelers • No contact between enhancer bound proteins and the target promoter • Open a chromatin domain but not target a promoter • Linking via enhancer-facilitators

  3. Direct contact in activation • Demonstrated in bacteria and yeast (some genes) • Upstream activation sequences are adjacent to minimal promoters • Examples • lambda repressor activates RNA polymerase at PRM. • cAMP-CAP activates RNA polymerase at lac. Direct contact between cAMP-CAP and the C-treminal domain of the alpha subunit of RNA polymerase

  4. Suppression is strong evidence for direct contact • Hypothesis: an AD makes direct contact with a component of the transcriptional apparatus • Prediction: LOF mutations in the activation domain should be suppressed by appropriate mutations in that component. • E.g. mutations in CAP can be suppressed by mutation in the a subunit of RNA Pol. CTD

  5. How do distal enhancers work?

  6. Does activation require communication between an enhancer and a promoter? • If so, expect • An effect on rate of transcription • Specific binding between activator or co-activator and the transcription complex • Mutations in target of binding should abolish activation • Find targets in suppressor screens • If so, is it by looping vs. tracking? • Direct interaction? • Interact via another component? • Tracking?

  7. Some enhancers increase the rate of transcription initiation Polymerase density and amount of transcription increases in all cells in a population

  8. Looping vs. tracking • Communication between enhancer and promoter can be via direct contact • Contact between proteins bound to adjacent sites • Contact between proteins at distal sites, with DNA between them looped out. • Communication can be via tracking • Some component(s) of the transcriptional apparatus enter the chromosome at an enhancer and move along (track) until they act at a distal promoter.

  9. Pol IIa Direct contact for activation Enhancer IID PolII Promoter GTIF? Coactivator?

  10. Tracking for activation Enhancer PolII IID Promoter

  11. Interactions may be facilitated by DNA-bending proteins • Many proteins that bind in the minor groove of DNA also bend the DNA. • TBP, YY1, HMG I(Y) • interferon-b gene enhancer • binding sites for 3 conventional txn factors • binding sites for HMG I(Y) • requires binding and bending of DNA by HMGI(Y) for activation by the other proteins bound to the enhancer.

  12. Interferon beta Enhancer-Promoter

  13. Can activation occur without communication between an enhancer and a promoter? • If so, expect no specific binding between activator and the transcription complex • Possible models: • Open a chromatin domain so that it is more likely to be expressed • Affect probability that gene is in a transcriptionally competent region

  14. Some enhancers increase the probability that a gene is in a transcriptionally competent region With enhancer Increase in fraction of cells expressing the reporter gene. Amount of expression per expressing cell is same with and without enhancer. Without enhancer

  15. Experiments to look for targets of activators

  16. What proteins bind to the activation domain? • Use affinity chromatography, with AD as the ligand • Determine the nuclear proteins that bind specifically to that activation domain. • Find that some GTFs, especially TAFs, bind to either acidic or Q-rich ADs • E.g. the acidic AD of VP16 will bind to TBP, TAFII40 and TFIIB • Q-rich AD of Sp1 binds TAFII130

  17. IIA IIE TAFs } TFIID TBP IIB IIE IIA Pol IIa IIB Inr TBP GTIFs for RNA polymerase II Modulates helicase Helicase helicase IIF IIH Targets Pol II to promoter Recognize core promoter CTD protein kinase protein kinase IIF IIH CTD of large subunit of Pol II Many GTIFs are possible targets for activators of transcription.

  18. GTIFs can be targets of activation domains in vitro 130

  19. Are TAFs required for transcriptional activation? • Construct conditional (ts) loss-of-function (LOF) alleles in genes for TAFs in yeast. • Examine the level of expression of various target genes before and after temperature shift (active vs. inactive TAF). • See that many genes are still activated in the absence of TAF function! • TAFS are notrequired for allactivation. • TAFs are important - LOF alleles are lethal. Other functions include cell cycle progression.

  20. Co-regulators • Some sequence-specific activators (or repressors) do not regulate transcription by themselves. • Sp1 + TBP + RNA Pol II + other GTFs + promoter DNA: only basal transcription • Co-activators and co-repressors are also needed • Sp1 + TBP + TAFS + RNA Pol II + other GTFs + promoter DNA: get activated transcription

  21. Activators and Co-rgulators Lemon & Tjian (2000) Genes & Devel. 14:2551

  22. Mediator is a co-activator • Yeast RNA Pol II does not respond to activators, but the RNA Pol II holoenzyme does respond to activators • Mediator (SRBs, Rgr1, Gal11, Med 1, 2, 6, 7, etc) is a type of co-activator

  23. Some co-regulators work on chromatin • Transcriptional activation in vitro from some promoters requires a chromatin template • Some co-activators and co-repressors covalently modify histones and transctipion factors: • Acetyl transferases (co-activators) • Deacetylases (co-repressors) • Kinases, Methylases, ADP-ribosyltransferases • Some co-activators use ATP hydrolysis to modify nucleosomes • SWI/SNF, ISWI, etc

  24. Classes of co-regulators • Class I: activator and repressor targets in polymerase and GTIFs • TAFs, TFIID • Adapters that bind to the activators • VP16, OCA-B • Mediator • SRBs, etc. 3 in mammals: CRSP, SRC, NAT • Complexes that covalently modify nucleosomal histones and transcription factors • HATS, HDACs, kinases, methyl transferases, etc • Complexes that remodel chromatin in an ATP-dependent manner: SWI/SNF

  25. Regulating the regulators

  26. Regulation of activator proteins • Tissue-specific synthesis of activator proteins • Covalent modification • Phosphorylation of HSTF will activate it. • Phosphorylation of AP1 at some sites will activate it, at other sites will inhibit it. • Some transcription factors are activated by acetylation. • Active form of the transcription factor can be imported to the nucleus after dissociation of an inhibitor in cytoplasm • Exchange heterodimeric partners

  27. Example of steroid-hormone receptors • In the absence of ligand (steroid), the receptor is in an inactive form in the cytoplasm. • Complexed with Hsp90 and other proteins. • When steroid binds, Hsp90 dissociates, and the hormone-receptor complex is imported into the nucleus. • In the nucleus, the hormone-receptor complex associates with an additional protein, binds to specific sites and activates target genes.

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